P.O. VOX
K-Number: K860993 · 1986-04-25
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Device Summary
Frequently Asked Questions
What is the P.O. VOX?
P.O. VOX is a medical device that received FDA 510(k) clearance on 1986-04-25. The listed applicant is Bloomfield Research and Development, Inc.. The 510(k) number is K860993.
When did P.O. VOX receive FDA 510(k) clearance?
P.O. VOX received FDA 510(k) clearance on 1986-04-25, under 510(k) number K860993.
Who is the listed applicant for P.O. VOX?
The FDA 510(k) record lists Bloomfield Research and Development, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for P.O. VOX?
The FDA product code for P.O. VOX is ESE.
Other records listing Bloomfield Research and Development, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: ESE)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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